FI103888B - Analoginen menetelmä valmistaa terapeuttisesti aktiivista akridiinijohdannaista - Google Patents

Analoginen menetelmä valmistaa terapeuttisesti aktiivista akridiinijohdannaista

Info

Publication number
FI103888B
FI103888B FI933149A FI933149A FI103888B FI 103888 B FI103888 B FI 103888B FI 933149 A FI933149 A FI 933149A FI 933149 A FI933149 A FI 933149A FI 103888 B FI103888 B FI 103888B
Authority
FI
Finland
Prior art keywords
group
4alkoxy
4alkyl
hydrogen atom
atom
Prior art date
Application number
FI933149A
Other languages
English (en)
Finnish (fi)
Swedish (sv)
Other versions
FI933149L (fi
FI103888B1 (fi
FI933149A0 (fi
Inventor
Bernard Andre Dumaitre
Nerina Dodic
Original Assignee
Glaxo Lab Sa
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from GB919100637A external-priority patent/GB9100637D0/en
Priority claimed from GB919100628A external-priority patent/GB9100628D0/en
Priority claimed from GB919115956A external-priority patent/GB9115956D0/en
Priority claimed from GB919115981A external-priority patent/GB9115981D0/en
Application filed by Glaxo Lab Sa filed Critical Glaxo Lab Sa
Publication of FI933149L publication Critical patent/FI933149L/fi
Publication of FI933149A0 publication Critical patent/FI933149A0/fi
Application granted granted Critical
Publication of FI103888B1 publication Critical patent/FI103888B1/fi
Publication of FI103888B publication Critical patent/FI103888B/fi

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C205/00Compounds containing nitro groups bound to a carbon skeleton
    • C07C205/07Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by halogen atoms
    • C07C205/11Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by halogen atoms having nitro groups bound to carbon atoms of six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C205/00Compounds containing nitro groups bound to a carbon skeleton
    • C07C205/13Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups
    • C07C205/26Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups and being further substituted by halogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C205/00Compounds containing nitro groups bound to a carbon skeleton
    • C07C205/27Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups
    • C07C205/35Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
    • C07C205/36Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton to carbon atoms of the same non-condensed six-membered aromatic ring or to carbon atoms of six-membered aromatic rings being part of the same condensed ring system
    • C07C205/37Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton to carbon atoms of the same non-condensed six-membered aromatic ring or to carbon atoms of six-membered aromatic rings being part of the same condensed ring system the oxygen atom of at least one of the etherified hydroxy groups being further bound to an acyclic carbon atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C205/00Compounds containing nitro groups bound to a carbon skeleton
    • C07C205/49Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups
    • C07C205/56Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups having nitro groups bound to carbon atoms of six-membered aromatic rings and carboxyl groups bound to acyclic carbon atoms of the carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D219/00Heterocyclic compounds containing acridine or hydrogenated acridine ring systems
    • C07D219/04Heterocyclic compounds containing acridine or hydrogenated acridine ring systems with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the ring system
    • C07D219/06Oxygen atoms

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)
  • Dry Shavers And Clippers (AREA)
  • Soft Magnetic Materials (AREA)
  • Paper (AREA)
  • Laminated Bodies (AREA)
FI933149A 1991-01-11 1993-07-09 Analoginen menetelmä valmistaa terapeuttisesti aktiivista akridiinijohdannaista FI103888B (fi)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
GB919100637A GB9100637D0 (en) 1991-01-11 1991-01-11 Chemical compounds
GB919100628A GB9100628D0 (en) 1991-01-11 1991-01-11 Chemical compounds
GB919115956A GB9115956D0 (en) 1991-07-24 1991-07-24 Chemical compounds
GB919115981A GB9115981D0 (en) 1991-07-24 1991-07-24 Chemical compounds
PCT/EP1992/000020 WO1992012132A1 (en) 1991-01-11 1992-01-07 Acridine derivatives

Publications (4)

Publication Number Publication Date
FI933149L FI933149L (fi) 1993-07-09
FI933149A0 FI933149A0 (fi) 1993-07-09
FI103888B1 FI103888B1 (fi) 1999-10-15
FI103888B true FI103888B (fi) 1999-10-15

Family

ID=27450605

Family Applications (1)

Application Number Title Priority Date Filing Date
FI933149A FI103888B (fi) 1991-01-11 1993-07-09 Analoginen menetelmä valmistaa terapeuttisesti aktiivista akridiinijohdannaista

Country Status (25)

Country Link
US (1) US5604237A (cs)
EP (2) EP0494623A1 (cs)
JP (1) JP2783680B2 (cs)
KR (1) KR100220538B1 (cs)
AT (1) ATE153660T1 (cs)
AU (1) AU652996B2 (cs)
CA (1) CA2100258C (cs)
CZ (1) CZ283038B6 (cs)
DE (1) DE69220037T2 (cs)
DK (1) DK0569380T3 (cs)
ES (1) ES2104887T3 (cs)
FI (1) FI103888B (cs)
GE (1) GEP20002210B (cs)
GR (1) GR3024525T3 (cs)
HU (2) HUT68856A (cs)
IE (1) IE920083A1 (cs)
IL (1) IL100631A (cs)
MX (1) MX9200109A (cs)
NO (1) NO300267B1 (cs)
NZ (1) NZ241278A (cs)
PL (1) PL168202B1 (cs)
RU (1) RU2119482C1 (cs)
SG (1) SG45403A1 (cs)
SK (1) SK280864B6 (cs)
WO (1) WO1992012132A1 (cs)

Families Citing this family (48)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE153660T1 (de) * 1991-01-11 1997-06-15 Glaxo Lab Sa Acridinderivate
TR28930A (tr) * 1992-05-07 1997-07-21 Zeneca Ltd Alkil sübstitüentli nitrotoluen türevleri
GB9209872D0 (en) * 1992-05-07 1992-06-24 Ici Plc Alkyl substituted nitrotoluene derivatives
DE69310367T2 (de) * 1992-07-10 1997-08-14 Glaxo Lab Sa Anilide-derivate
RU2036198C1 (ru) * 1993-04-01 1995-05-27 Товарищество с ограниченной ответственностью "Полисан" N-МЕТИЛ-N-( α,D -ГЛЮКОПИРАНОЗИЛ) АММОНИЯ-2-(АКРИДОН-9-ОН-10-ИЛ)АЦЕТАТ(ЦИКЛОФЕРОН), ОБЛАДАЮЩИЙ ИНТЕРФЕРОНОГЕННОЙ, ПРОТИВОВИРУСНОЙ, В ТОМ ЧИСЛЕ АНТИВИЧ, АНТИПАРАЗИТАРНОЙ, АНТИПРОМОТОРНОЙ И РАДИОПРОТЕКТИВНОЙ АКТИВНОСТЬЮ
US5387685A (en) * 1993-07-16 1995-02-07 American Cyanamid Co MDR reversal agents
DE4422517A1 (de) * 1994-06-28 1996-01-04 Dresden Arzneimittel Neue (2-(3,4-Dimethoxy-phenyl)-ethyl)-(2-phenoxy-ethyl)-amine, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel
DE69531691T2 (de) * 1994-08-04 2004-07-08 C & C Research Labs Neues amin-derivat, verfahren zur herstellung und dessen verwendung als anti-arrhythmisches mittel
CA2201628A1 (en) * 1994-10-05 1996-04-18 Wei-Qin Tong Parenteral pharmaceutical compositions containing gf120918a
FR2726267B1 (fr) * 1994-10-26 1998-01-02 Smithkline Beecham Lab Nouveaux agents anti-arythmiques, compositions pharmaceutiques les contenant, et procede pour les preparer
US6395770B1 (en) 1995-10-26 2002-05-28 Baker Norton Pharmaceuticals, Inc. Method and compositions for administering taxanes orally to human patients
US6245805B1 (en) 1995-10-26 2001-06-12 Baker Norton Pharmaceuticals, Inc. Method, compositions and kits for increasing the oral bioavailability of pharmaceutical agents
AU1597197A (en) * 1996-02-01 1997-08-22 Byk Gulden Lomberg Chemische Fabrik Gmbh Thienoquinolines
US6713517B1 (en) 1996-03-08 2004-03-30 Oxigene, Inc. Use of aryl N-substituted carboxamides directly and as radio-and chemosensitizers for killing tumor and cancer cells and novel compounds for such use
RU2118532C1 (ru) * 1996-04-10 1998-09-10 Олег Викторович Травкин Противоинфекционное, противовоспалительное и противоопухолевое лекарственное средство
MY118642A (en) * 1996-10-18 2004-12-31 Xenova Ltd Anthranilic acid derivatives as multi drug resistance modulators
CZ135199A3 (cs) * 1996-10-18 1999-09-15 Xenova Limited Způsob přípravy N-/2-(dimethylamino)ethyl/akridin-4-karboxyamidu
GB9708805D0 (en) 1997-05-01 1997-06-25 Smithkline Beecham Plc Compounds
GB9710612D0 (en) * 1997-05-23 1997-07-16 Glaxo Group Ltd Synthesis of acridine derivatives
SK157599A3 (en) * 1997-05-27 2002-10-08 Baker Norton Pharma Method and compositions for administering taxanes orally to human patients
GB9718903D0 (en) * 1997-09-05 1997-11-12 Glaxo Group Ltd Method,compositions and kits for increasing the oral bioavailability of pharmaceutical agents
GB9810876D0 (en) 1998-05-20 1998-07-22 Smithkline Beecham Plc Compounds
GB9812189D0 (en) * 1998-06-05 1998-08-05 Glaxo Group Ltd Methods and compositions for increasing penetration of HIV protease inhibitors
AU4698299A (en) * 1998-06-30 2000-01-17 Du Pont Pharmaceuticals Company 5-HT7 receptor antagonists
RU2135474C1 (ru) * 1998-08-19 1999-08-27 Травкин Олег Викторович Соли 1-дезокси-1-n-метиламиногексаспиртов с n-акридонуксусной кислотой, обладающие иммуномодулирующей активностью, и лекарственное средство на их основе
EP1119563B1 (en) 1998-10-08 2006-02-01 SmithKline Beecham plc Tetrahydrobenzazepine derivatives useful as modulators of dopamine d3 receptors (antipsychotic agents)
GB9824579D0 (en) * 1998-11-10 1999-01-06 Novartis Ag Organic compounds
AU4955200A (en) 1999-05-17 2000-12-05 Cancer Research Ventures Limited A method of improving bioavailability of orally administered drugs, a method of screening for enhancers of such bioavailability and novel pharmaceutical compositions for oral delivery of drugs
EP2289549A3 (en) 1999-10-01 2011-06-15 Immunogen, Inc. Immunoconjugates for treating cancer
US6521635B1 (en) 2000-01-20 2003-02-18 The United States Of America As Represented By The Department Of Health And Human Services Inhibition of MXR transport by acridine derivatives
PT1261325E (pt) 2000-02-18 2010-12-10 New York Medical College Composições inibidoras de tumores que incluem nitroacridinas
US6703392B2 (en) * 2000-03-14 2004-03-09 Actelion Pharmaceuticals Ltd. 1,2,3,4-tetrahydroisoquinoline derivatives
EP1288202A4 (en) 2000-05-11 2003-07-02 Banyu Pharma Co Ltd N-acyltetrahydroisoquinoline derivatives
CN1469735A (zh) * 2000-10-16 2004-01-21 ����˹��ҩ�﹫˾ 米托蒽醌的脂质体制剂
EP1506188B1 (en) * 2002-05-14 2009-02-25 Xenova Limited Process for the preparation of a hydrate of an anthranilic acid derivative
RU2279873C2 (ru) * 2002-05-31 2006-07-20 Ар.Пи.ШЕРЕР ТЕКНОЛОДЖИЗ, ИНК. Пероральная фармацевтическая композиция для мягких капсул, содержащая винорелбин, и способ лечения
WO2004039795A2 (en) * 2002-10-29 2004-05-13 Fujisawa Pharmaceutical Co., Ltd. Amide compounds for the treatment of hyperlipidemia
BRPI0508263B8 (pt) 2004-03-01 2021-05-25 Idorsia Pharmaceuticals Ltd derivados de 1, 2, 3, 4-tetra-hidro-isoquinolina, composição farmacêutica, e, uso de derivado de 1, 2, 3, 4-tetra-hidro-isoquinolina
RU2326115C2 (ru) * 2005-11-21 2008-06-10 Ефаг АО Соли 1-алкиламино-1-дезоксиполиолов с 9-оксоакридин-10-уксусной кислотой, лекарственные препараты на их основе, применение, способы профилактики и лечения
BRPI0709049A2 (pt) * 2006-03-22 2011-06-21 Janssen Pharmaceutica Nv composto inibidor da interação entre mdm2 e p53, composição farmacêutica, processo para preparar a referida composição farmacêutica, uso do composto, combinação, e processo para preparar o referido composto
RU2346691C2 (ru) * 2007-03-29 2009-02-20 Ефаг АО Применение 9-оксоакридин-10-уксусной кислоты и/или ее соли в комбинации с антиэстрогеном и/или прогестином для лечения эстрогензависимых опухолей, способ лечения и наборы
RU2346692C2 (ru) * 2007-03-29 2009-02-20 Ефаг АО Применение 9-оксоакридин-10-уксусной кислоты, ее солей и сложных эфиров в комбинированной терапии рака яичников, способ лечения и наборы
SE531698C2 (sv) * 2007-07-12 2009-07-07 Respiratorius Ab Nya bronkdilaterande a,b-omättade amider
WO2015142670A1 (en) * 2014-03-15 2015-09-24 Medisyn Technologies, Inc. Anti-diabetic compounds, pharmaceutical compositions containing them, and method to treat diabetes
CN104434808A (zh) 2014-07-03 2015-03-25 石药集团中奇制药技术(石家庄)有限公司 一种治疗性纳米粒子及其制备方法
KR20200134257A (ko) * 2018-03-21 2020-12-01 이즈미 테크놀로지 엘엘씨 엘라크리다의 중수소화 유사체
CN115385847B (zh) * 2021-06-15 2023-09-29 山东第一医科大学(山东省医学科学院) 多取代二芳基类化合物及其制备方法和应用
CN117414367A (zh) * 2022-08-09 2024-01-19 北京清华长庚医院 一种逆转仑伐替尼耐药的药物组合物及其用途

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4250182A (en) * 1972-02-24 1981-02-10 Burroughs Wellcome Co. Pharmaceutical composition containing acridone compounds and method of using same
US4021551A (en) * 1972-06-07 1977-05-03 Boehringer Ingelheim Gmbh 3,6-Bis-(heterocyclic aminoacyl-amino)-acridines and salts thereof
US4127573A (en) * 1972-09-06 1978-11-28 Burroughs Wellcome Co. Ditetrazole substituted acridone compounds
ATE12779T1 (de) * 1980-09-30 1985-05-15 Bayer Ag Verfahren zur herstellung eines antithrombinheparin-komplexes sowie diesen komplex enthaltende pharmazeutische mischungen.
NZ198115A (en) * 1981-08-21 1985-05-31 New Zealand Dev Finance 9-anilinoacridines;pharmaceutical compositions
NZ201084A (en) * 1982-06-25 1985-10-11 New Zealand Dev Finance 4-carboxamidoacridine derivatives and pharmaceutical compositions containing such
IN164921B (cs) * 1986-07-22 1989-07-08 Hoechst India
US5104858A (en) * 1988-09-29 1992-04-14 Yale University Sensitizing multidrug resistant cells to antitumor agents
CA1340821C (en) * 1988-10-06 1999-11-16 Nobuyuki Fukazawa Heterocyclic compounds and anticancer-drug reinforcing agents containing them as effective components
IE902182A1 (en) * 1989-06-19 1991-01-02 Wellcome Found Medicaments
ATE153660T1 (de) * 1991-01-11 1997-06-15 Glaxo Lab Sa Acridinderivate
US5296602A (en) * 1991-03-18 1994-03-22 Sloan-Kettering Institute For Cancer Research Multisubstituted 1-hydroxy-9-acridones with anticancer activity
US5240936A (en) * 1992-05-14 1993-08-31 Texas A&M University System Treating or preventing ocular inflammation or systemic imflammatory disease

Also Published As

Publication number Publication date
IL100631A0 (en) 1992-09-06
SG45403A1 (en) 1998-01-16
SK280864B6 (en) 2000-08-14
WO1992012132A1 (en) 1992-07-23
DE69220037D1 (de) 1997-07-03
EP0569380A1 (en) 1993-11-18
MX9200109A (es) 1992-09-01
DE69220037T2 (de) 1997-11-06
ATE153660T1 (de) 1997-06-15
EP0569380B1 (en) 1997-05-28
CA2100258C (en) 1999-12-14
IE920083A1 (en) 1992-07-15
PL168202B1 (pl) 1996-01-31
IL100631A (en) 1996-09-12
FI933149L (fi) 1993-07-09
HU211623A9 (en) 1995-12-28
NO932512D0 (no) 1993-07-09
EP0494623A1 (en) 1992-07-15
SK73093A3 (en) 1994-01-12
NZ241278A (en) 1994-05-26
AU652996B2 (en) 1994-09-15
JP2783680B2 (ja) 1998-08-06
FI103888B1 (fi) 1999-10-15
GEP20002210B (en) 2000-08-25
AU1154392A (en) 1992-08-17
CA2100258A1 (en) 1992-07-12
HU9301989D0 (en) 1993-10-28
US5604237A (en) 1997-02-18
CZ137893A3 (en) 1994-02-16
CZ283038B6 (cs) 1997-12-17
HUT68856A (en) 1995-08-28
FI933149A0 (fi) 1993-07-09
NO932512L (no) 1993-09-09
NO300267B1 (no) 1997-05-05
JPH06506440A (ja) 1994-07-21
GR3024525T3 (en) 1997-11-28
KR100220538B1 (ko) 1999-09-15
DK0569380T3 (da) 1997-12-22
RU2119482C1 (ru) 1998-09-27
ES2104887T3 (es) 1997-10-16

Similar Documents

Publication Publication Date Title
FI103888B (fi) Analoginen menetelmä valmistaa terapeuttisesti aktiivista akridiinijohdannaista
DE69418704D1 (de) Anthranilsäure derivate
ATE172201T1 (de) Morphinan-derivate und medizinische verwendung
NO930774D0 (no) Baccatin-iii-derivater
EP1035123A4 (en) NEW HETEROCYCLIC COMPOUNDS
FI940414A0 (fi) Kinoliini- tai kinatsoliinijohdannaiset, niiden valmistus ja käyttö
DE69120581D1 (de) 1,8-Naphthyridin-2-on-Derivate
NO931317D0 (no) Et terapeutisk middel for parkinson's sykdom
DE69122427D1 (de) Imidazonaphthyridinderivate
ATE182331T1 (de) Oxazolidone derivative als monoamine- oxidaseinhibitoren
FR2696465B1 (fr) Nouveaux dérivés d'ellipticine, leur procédé de préparation et les compositions pharmaceutiques qui les contiennent.
DE60045821D1 (de) Derivate von aromatische heterocyclen enthaltende integraseinhibitoren
ATE205209T1 (de) Chinolincarbonsäurederivate und ihre salze
ZA917141B (en) 3-(1h-indazol-3-yl)-4-pyridinamines,a process and intermediates for their preparation and their use as medicaments
ATE125807T1 (de) Flavonderivate.
ES8504712A1 (es) Un procedimiento para preparar nuevas dihidropiridinas
MY110626A (en) Acridine derivatives